TN-RDAC To Inform TennCARE On Pharmaceutical Treatments

Wednesday, May 12, 2021
The newly formed Tennessee Rare Disease Advisory Council or TN-RDAC (pronounced AHR-dak) has set its priorities to advocate for Tennesseans diagnosed with rare diseases, including advising TennCare’s Pharmacy Advisory Committee and Drug Utilization Review Committee on pharmaceutical treatments, as well as identifying the overall impact of rare diseases on Tennesseans.
 
Created by public charter in the 111th Tennessee General Assembly, TN-RDAC elected at its inaugural meeting its Chairman Dr.
Scott Strome, executive dean of the University of Tennessee College of Medicine and vice chancellor for clinical affairs at UT Health Science Center. Dr. Strome brings rare disease research and clinical experience to the TN-RDAC. 
 
The legislation that enabled Tennessee’s RDAC was sponsored by Sen. Shane Reeves and Rep. David Hawk, and was signed into law by Governor Bill Lee in 2020. 
 
“Tennessee’s RDAC is comprised of a panel of experts who can advise us on treatments for some of the most challenging medical situations,” said Senator Reeves. “We look forward to the Council helping us to better treat patients in the most efficient and effective manner as today’s science knows.”
 
TN-RDAC is beginning its work by conducting a survey to learn more about the needs of individuals, families and loved ones affected by rare diseases in the state. The Council calls on all affected individuals to take the survey at https://tnrdac.org/activities/tennessee-survey/. 
 
TN-RDAC elected officers also include Vice Chairperson Terry Jo Bichell, RN, MPH, PhD, a neuroscience researcher and Tennessee state ambassador for the Rare Action Network of the National Organization for Rare Disorders. Dr. Bichell is also founder and director of COMBINEDBrain, a consortium of patient advocates, clinicians, researchers and pharmaceutical companies supporting the development of treatments for unmet medical needs. Gillian Hooker, PhD, ScM, CGC chief scientific officer of Concert Genetics, and past-president of the National Society of Genetic Counselors, will serve as the TN-RDAC secretary.
 
TN-RDAC members were appointed by Governor Bill Lee, Lt. Governor Randy McNally and Speaker of the House Cameron Sexton. Additional members include: 
 
J. Clay Callison, MD, pulmonary medicine, vice president and chief medical information officer, UT Medical Center; director, Adult Cystic Fibrosis Center, UT Medical Center
Eugene “Chip” Chambers, MD, assistant clinical professor of surgery, Vanderbilt University Medical Center; founder and president, DADA2Foundation, a patient advocacy group
Reginald French, president and chief executive officer, the Sickle Cell Foundation of Tennessee
Rizwan Hamid, MD, PhD, director, Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine
Suzanne Jackowski, PhD, member, Department of Infectious Diseases, St. Jude Children’s Research Hospital 
Megan Crow, BSN, flight nurse, Vanderbilt LifeFlight; co-chair of the advocacy committee, Tennessee Hemophilia and Bleeding Disorders Foundation
Kim Stephens, DBA, a communications, diversity and inclusion consultant; president and chief executive officer, Project Alive, a patient advocacy organization committed to finding and funding a cure for Hunter Syndrome
Lora Underwood, PharmD, director of clinical pharmacy services, Bureau of TennCare
 
“I am honored to serve with such an esteemed group,” said Dr. Strome. “We have a unique opportunity to advise TennCare on how to help some of our most vulnerable patients find and receive the best treatments available while being mindful about the need to be good stewards of taxpayer dollars.”
 
Officials said, "A rare disease is defined as a disease that affects fewer than 200,000 people. There are 7,000 known rare diseases affecting approximately 30 million men, women and children in the United States. While the exact causes for many rare diseases remain unknown, 80 percent of rare diseases are genetic in origin and can be linked to mutations in a single gene or in multiple genes, which can be passed down from generation to generation. 
 
"Persons with rare diseases often face challenges including delays in obtaining a diagnosis, misdiagnosis, shortages of medical specialists who can provide treatment and lack of access to therapies and medication used to treat rare diseases. Researchers have made considerable progress in developing diagnostic tools and treatment protocols as well as in discovering methods of prevention and treatment, but much more remains in the search for new therapies."

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